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26 results found for "DNA amount" in all classes.

Competent host में excessive DNA amount क्यों problem हो सकता है?

Why can excessive DNA amount be a problem in a competent host?

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A. Cells stress हो सकती हैंCells can be stressed

Step 1

Concept

Too much DNA or impurities can stress cells. An optimal DNA amount is better.

Step 2

Why this answer is correct

The correct answer is A. Cells stress हो सकती हैं / Cells can be stressed. Too much DNA or impurities can stress cells. An optimal DNA amount is better.

Step 3

Exam Tip

बहुत अधिक DNA या impurities cells पर stress डाल सकते हैं। Optimal DNA amount better होता है।

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Plasmid DNA की मात्रा बहुत अधिक होने पर क्या समस्या हो सकती है?

What problem can occur if plasmid DNA amount is too high?

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Correct Answer

C. Cells stress हो सकती हैं और efficiency घट सकती हैCells may get stressed and efficiency may decrease

Step 1

Concept

Excess DNA or impurities can stress cells. An optimal amount is better for transformation efficiency.

Step 2

Why this answer is correct

The correct answer is C. Cells stress हो सकती हैं और efficiency घट सकती है / Cells may get stressed and efficiency may decrease. Excess DNA or impurities can stress cells. An optimal amount is better for transformation efficiency.

Step 3

Exam Tip

Excess DNA या impurities cells को stress कर सकती हैं। Optimal amount transformation efficiency के लिए बेहतर होता है।

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प्रतिबंध एंजाइम प्रयोग में डीएनए की मात्रा बहुत कम हो तो क्या समस्या हो सकती है?

What problem can occur if DNA amount is very low in a restriction enzyme experiment?

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Correct Answer

A. खंडों को देखना कठिन हो सकता हैIt may be difficult to see fragments

Step 1

Concept

With little DNA the bands may look weak. Adequate sample is important in experiments.

Step 2

Why this answer is correct

The correct answer is A. खंडों को देखना कठिन हो सकता है / It may be difficult to see fragments. With little DNA the bands may look weak. Adequate sample is important in experiments.

Step 3

Exam Tip

कम डीएनए से बैंड कमजोर दिख सकते हैं। प्रयोग में पर्याप्त नमूना महत्वपूर्ण होता है।

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यदि DNA sample में RNA contamination हो तो restriction digestion पर सामान्यतः सबसे बड़ा effect क्या होगा?

If a DNA sample has RNA contamination what is generally the main effect on restriction digestion?

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Correct Answer

B. accurate DNA quantification confuse हो सकती हैAccurate DNA quantification can be confused

Step 1

Concept

RNA contamination can affect DNA amount estimation. RNase treatment or cleanup can help.

Step 2

Why this answer is correct

The correct answer is B. accurate DNA quantification confuse हो सकती है / Accurate DNA quantification can be confused. RNA contamination can affect DNA amount estimation. RNase treatment or cleanup can help.

Step 3

Exam Tip

RNA contamination DNA amount estimate को प्रभावित कर सकती है। RNase treatment या cleanup helpful हो सकता है।

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Restriction enzyme unit reaction planning में कैसे उपयोगी है?

How is restriction enzyme unit useful in reaction planning?

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Correct Answer

B. enzyme activity amount estimate करने मेंIn estimating enzyme activity amount

Step 1

Concept

Units describe enzyme activity in a standard way. Units are chosen according to DNA amount.

Step 2

Why this answer is correct

The correct answer is B. enzyme activity amount estimate करने में / In estimating enzyme activity amount. Units describe enzyme activity in a standard way. Units are chosen according to DNA amount.

Step 3

Exam Tip

Units enzyme activity को standard way में बताते हैं। DNA amount के अनुसार units चुने जाते हैं।

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Restriction fragment analysis में band intensity से क्या rough information मिल सकती है?

What rough information can band intensity give in restriction fragment analysis?

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Correct Answer

A. DNA amount in band का अनुमानEstimate of DNA amount in band

Step 1

Concept

Band brightness is related to DNA mass. It gives a rough estimate but not exact quantification.

Step 2

Why this answer is correct

The correct answer is A. DNA amount in band का अनुमान / Estimate of DNA amount in band. Band brightness is related to DNA mass. It gives a rough estimate but not exact quantification.

Step 3

Exam Tip

Band brightness DNA mass से जुड़ी होती है। यह exact quantification नहीं पर rough estimate देती है।

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Restriction digestion में sample concentration normalize क्यों करते हैं?

Why is sample concentration normalized in restriction digestion?

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Correct Answer

A. different reactions में equal DNA amount रखने के लिएTo keep equal DNA amount in different reactions

Step 1

Concept

Equal DNA amount makes comparison fair. This improves interpretation of gel band intensity.

Step 2

Why this answer is correct

The correct answer is A. different reactions में equal DNA amount रखने के लिए / To keep equal DNA amount in different reactions. Equal DNA amount makes comparison fair. This improves interpretation of gel band intensity.

Step 3

Exam Tip

Equal DNA amount comparison को fair बनाता है। इससे gel band intensity interpretation बेहतर होती है।

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Restriction digestion के लिए DNA quantification क्यों किया जाता है?

Why is DNA quantification done for restriction digestion?

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Correct Answer

A. enzyme और DNA amount सही रखने के लिएTo keep enzyme and DNA amount correct

Step 1

Concept

Knowing DNA amount helps set enzyme units and reaction correctly. This makes digestion reliable.

Step 2

Why this answer is correct

The correct answer is A. enzyme और DNA amount सही रखने के लिए / To keep enzyme and DNA amount correct. Knowing DNA amount helps set enzyme units and reaction correctly. This makes digestion reliable.

Step 3

Exam Tip

DNA amount जानकर enzyme units और reaction setup सही किया जाता है। इससे digestion reliable होती है।

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Very faint bands का common कारण क्या हो सकता है?

What can be a common reason for very faint bands?

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Correct Answer

A. low DNA amount

Step 1

Concept

Low DNA loading can give faint bands. Check sample concentration and loading amount.

Step 2

Why this answer is correct

The correct answer is A. low DNA amount. Low DNA loading can give faint bands. Check sample concentration and loading amount.

Step 3

Exam Tip

कम DNA loading faint bands दे सकती है। Sample concentration और loading amount देखें।

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Restriction digest में DNA loading बहुत अधिक हो तो क्या समस्या हो सकती है?

What problem can occur if too much DNA is loaded in restriction digest gel?

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Correct Answer

A. bands smear या distorted हो सकते हैंBands may smear or distort

Step 1

Concept

Overloading the gel can make band interpretation difficult. Load proper DNA amount.

Step 2

Why this answer is correct

The correct answer is A. bands smear या distorted हो सकते हैं / Bands may smear or distort. Overloading the gel can make band interpretation difficult. Load proper DNA amount.

Step 3

Exam Tip

Overloading gel band interpretation को कठिन बना सकता है। Proper DNA amount load करें।

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Restriction digestion में बहुत अधिक DNA डालने से क्या हो सकता है?

What can happen if too much DNA is added in restriction digestion?

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Correct Answer

A. enzyme insufficient होकर incomplete digestion दे सकता हैEnzyme may become insufficient and give incomplete digestion

Step 1

Concept

DNA amount should match enzyme capacity. Too much DNA can make complete digestion difficult.

Step 2

Why this answer is correct

The correct answer is A. enzyme insufficient होकर incomplete digestion दे सकता है / Enzyme may become insufficient and give incomplete digestion. DNA amount should match enzyme capacity. Too much DNA can make complete digestion difficult.

Step 3

Exam Tip

DNA amount enzyme capacity से match होना चाहिए। बहुत अधिक DNA complete digestion को कठिन कर सकता है।

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Restriction digestion के बाद band बहुत faint हो तो क्या कारण हो सकता है?

What can cause a very faint band after restriction digestion?

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Correct Answer

B. कम DNA amountLow DNA amount

Step 1

Concept

Low DNA loading gives faint bands. Check DNA concentration and loading amount.

Step 2

Why this answer is correct

The correct answer is B. कम DNA amount / Low DNA amount. Low DNA loading gives faint bands. Check DNA concentration and loading amount.

Step 3

Exam Tip

Low DNA loading से faint bands दिखते हैं। DNA concentration और loading amount check करें।

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Gel पर expected insert band नहीं दिखे तो क्या संभव है?

What is possible if expected insert band is not seen on gel?

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Correct Answer

A. insert absent या digestion failed हो सकता हैInsert may be absent or digestion failed

Step 1

Concept

Absence of expected band can indicate wrong clone partial digestion or low DNA amount. Confirm with controls.

Step 2

Why this answer is correct

The correct answer is A. insert absent या digestion failed हो सकता है / Insert may be absent or digestion failed. Absence of expected band can indicate wrong clone partial digestion or low DNA amount. Confirm with controls.

Step 3

Exam Tip

Expected band न होना wrong clone partial digestion या low DNA amount का संकेत हो सकता है। Controls से confirm करें।

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Restriction enzyme unit का अर्थ क्या है?

What does a restriction enzyme unit mean?

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Correct Answer

C. defined condition में DNA काटने की activity amountAmount of activity to cut DNA under defined condition

Step 1

Concept

Enzyme units describe activity. Enzyme amount is chosen according to DNA amount in reaction setup.

Step 2

Why this answer is correct

The correct answer is C. defined condition में DNA काटने की activity amount / Amount of activity to cut DNA under defined condition. Enzyme units describe activity. Enzyme amount is chosen according to DNA amount in reaction setup.

Step 3

Exam Tip

Enzyme units activity बताते हैं। Reaction setup में DNA amount के अनुसार enzyme मात्रा चुनी जाती है।

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DNA isolation report में कौन सी values लिखना useful है?

Which values are useful to write in a DNA isolation report?

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A. yield purity ratio और storage detailYield purity ratio and storage detail

Step 1

Concept

It is useful to record DNA amount purity ratios and storage condition in a report. This helps future use.

Step 2

Why this answer is correct

The correct answer is A. yield purity ratio और storage detail / Yield purity ratio and storage detail. It is useful to record DNA amount purity ratios and storage condition in a report. This helps future use.

Step 3

Exam Tip

Report में DNA amount purity ratios और storage condition लिखना useful है। इससे future use आसान होता है।

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DNA isolation में low template samples के लिए क्या practice useful है?

What practice is useful for low template samples in DNA isolation?

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A. low-bind tubes और careful pipettingLow-bind tubes and careful pipetting

Step 1

Concept

In low DNA amount sample loss is a major issue. Low-bind tubes and careful handling preserve recovery.

Step 2

Why this answer is correct

The correct answer is A. low-bind tubes और careful pipetting / Low-bind tubes and careful pipetting. In low DNA amount sample loss is a major issue. Low-bind tubes and careful handling preserve recovery.

Step 3

Exam Tip

Low DNA amount में sample loss बड़ा issue होता है। Low-bind tubes और careful handling recovery बचाते हैं।

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Forensic DNA samples में contamination control क्यों बहुत जरूरी है?

Why is contamination control very important in forensic DNA samples?

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Correct Answer

A. small DNA amounts में गलत profile आ सकता हैWrong profile can occur with small DNA amounts

Step 1

Concept

Forensic samples can have low DNA amount. Contamination can make the result wrong.

Step 2

Why this answer is correct

The correct answer is A. small DNA amounts में गलत profile आ सकता है / Wrong profile can occur with small DNA amounts. Forensic samples can have low DNA amount. Contamination can make the result wrong.

Step 3

Exam Tip

Forensic samples में DNA amount कम हो सकता है। Contamination result को गलत कर सकती है।

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Sample amount बहुत कम हो तो क्या समस्या हो सकती है?

What problem can occur if sample amount is too low?

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Correct Answer

A. DNA yield कम हो सकती हैDNA yield may be low

Step 1

Concept

Low sample amount can give less DNA. Careful recovery is needed for low-yield samples.

Step 2

Why this answer is correct

The correct answer is A. DNA yield कम हो सकती है / DNA yield may be low. Low sample amount can give less DNA. Careful recovery is needed for low-yield samples.

Step 3

Exam Tip

कम sample से DNA amount कम मिल सकता है। Low-yield samples में careful recovery जरूरी है।

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Gel electrophoresis से DNA quantity का क्या अनुमान मिल सकता है?

What quantity estimate can gel electrophoresis provide for DNA?

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Correct Answer

A. band intensity से approximate amountApproximate amount from band intensity

Step 1

Concept

Band intensity can be compared with a known ladder or standard for approximate DNA amount. It is a rough estimate.

Step 2

Why this answer is correct

The correct answer is A. band intensity से approximate amount / Approximate amount from band intensity. Band intensity can be compared with a known ladder or standard for approximate DNA amount. It is a rough estimate.

Step 3

Exam Tip

Known ladder या standard से band intensity compare कर approximate DNA amount देख सकते हैं। यह rough estimate है।

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Fluorometric DNA quantification absorbance से कब बेहतर हो सकता है?

When can fluorometric DNA quantification be better than absorbance?

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Correct Answer

D. specific double-stranded DNA amount जानना होWhen specific double-stranded DNA amount is needed

Step 1

Concept

Fluorometric methods can use DNA-specific dyes. This can be more specific among contaminants.

Step 2

Why this answer is correct

The correct answer is D. specific double-stranded DNA amount जानना हो / When specific double-stranded DNA amount is needed. Fluorometric methods can use DNA-specific dyes. This can be more specific among contaminants.

Step 3

Exam Tip

Fluorometric methods DNA-specific dyes use कर सकते हैं। यह contaminants के बीच अधिक specific हो सकता है।

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DNA isolation के बाद PCR से पहले क्या check करना चाहिए?

What should be checked before PCR after DNA isolation?

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A. DNA purity और concentrationDNA purity and concentration

Step 1

Concept

Correct DNA amount and purity are needed for PCR template. Contaminants can inhibit amplification.

Step 2

Why this answer is correct

The correct answer is A. DNA purity और concentration / DNA purity and concentration. Correct DNA amount and purity are needed for PCR template. Contaminants can inhibit amplification.

Step 3

Exam Tip

PCR template के लिए सही DNA amount और purity जरूरी हैं। Contaminants amplification रोक सकते हैं।

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Spectrophotometer DNA isolation के बाद किसलिए उपयोगी है?

Why is a spectrophotometer useful after DNA isolation?

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Correct Answer

D. DNA concentration और purity estimate करने के लिएTo estimate DNA concentration and purity

Step 1

Concept

A spectrophotometer estimates DNA amount and purity using absorbance reading. It is useful in quality control.

Step 2

Why this answer is correct

The correct answer is D. DNA concentration और purity estimate करने के लिए / To estimate DNA concentration and purity. A spectrophotometer estimates DNA amount and purity using absorbance reading. It is useful in quality control.

Step 3

Exam Tip

Spectrophotometer absorbance reading से DNA amount और purity का अनुमान देता है। यह quality control में useful है।

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DNA isolation के बाद PCR करने से पहले किस बात की जाँच उपयोगी है?

What is useful to check before doing PCR after DNA isolation?

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Correct Answer

A. DNA purity और concentrationDNA purity and concentration

Step 1

Concept

DNA amount and purity are important for PCR template. Contaminants can inhibit PCR.

Step 2

Why this answer is correct

The correct answer is A. DNA purity और concentration / DNA purity and concentration. DNA amount and purity are important for PCR template. Contaminants can inhibit PCR.

Step 3

Exam Tip

PCR template के लिए DNA amount और purity important हैं। Contaminants PCR inhibit कर सकते हैं।

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DNA sample में protein contamination क्यों समस्या है?

Why is protein contamination a problem in a DNA sample?

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Correct Answer

A. यह downstream reactions में बाधा डाल सकती हैIt can interfere with downstream reactions

Step 1

Concept

Protein contamination can affect enzyme reactions and purity readings. Protein removal is necessary.

Step 2

Why this answer is correct

The correct answer is A. यह downstream reactions में बाधा डाल सकती है / It can interfere with downstream reactions. Protein contamination can affect enzyme reactions and purity readings. Protein removal is necessary.

Step 3

Exam Tip

Protein contamination enzyme reactions और purity readings को प्रभावित कर सकती है। Protein removal जरूरी है।

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डीएनए purity जाँचने के लिए कौन सा उपकरण उपयोगी है?

Which instrument is useful to check DNA purity?

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Correct Answer

B. स्पेक्ट्रोफोटोमीटरSpectrophotometer

Step 1

Concept

A spectrophotometer estimates DNA amount and purity using absorbance. Link it with quality check.

Step 2

Why this answer is correct

The correct answer is B. स्पेक्ट्रोफोटोमीटर / Spectrophotometer. A spectrophotometer estimates DNA amount and purity using absorbance. Link it with quality check.

Step 3

Exam Tip

Spectrophotometer absorbance के आधार पर DNA amount और purity का अनुमान देता है। इसे quality check से जोड़ें।

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High efficiency competent cells कब जरूरी हैं?

When are high-efficiency competent cells needed?

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Correct Answer

B. जब DNA amount बहुत कम होWhen DNA amount is very low

Step 1

Concept

High-efficiency competent cells can be useful for low DNA amount or difficult ligation products.

Step 2

Why this answer is correct

The correct answer is B. जब DNA amount बहुत कम हो / When DNA amount is very low. High-efficiency competent cells can be useful for low DNA amount or difficult ligation products.

Step 3

Exam Tip

Low DNA amount या difficult ligation products के लिए high-efficiency competent cells useful हो सकती हैं।

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